Allele Registry

Canonical Allele Identifier: PA2499266243

Gene: SLC22A8 HGNC NCBI

ClinVar RCV:

RCV001620273

ClinVar Variation:

1232453

HGVS (amino-acid)	Matching Registered Transcripts
NP_004245.2:p.Ile305Phe	CA6059770 NM_004254.4:c.913A>T